Elevated cell-free serum DNA detected in patients with myocardial infarction

Background: Cell-free DNA is detectable in the circulation. Increased cell-free DNA has been detected in cancer patients and individuals with trauma. We want to know whether patients with myocardial infarction (MI) also have increased cell-free DNA in their blood. Methods: We used a QIAamp blood kit...

Full description

Saved in:
Bibliographic Details
Published inClinica chimica acta Vol. 327; no. 1; pp. 95 - 101
Main Authors Chang, Christine P.-Y, Chia, Rhu-Hsin, Wu, Tsu-Lan, Tsao, Kuo-Chien, Sun, Chien-Feng, Wu, James T
Format Journal Article
LanguageEnglish
Published Shannon Elsevier B.V 2003
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Background: Cell-free DNA is detectable in the circulation. Increased cell-free DNA has been detected in cancer patients and individuals with trauma. We want to know whether patients with myocardial infarction (MI) also have increased cell-free DNA in their blood. Methods: We used a QIAamp blood kit for DNA extraction from serum and the PicoGreen DNA kit for quantification. DNA patterns of serum DNA were established by gel electrophoresis on 2.5% metarphor gel. Results: The average serum DNA in MI patients ( N=55) was 511±398 ng/ml, more than 10-fold higher than normal (36.3±23.8 ng/ml, n=274). Patients with increased CK-MB (>4%) were associated with highly increased concentrations of cell-free DNA (93.4%). There was no correlation between the concentration of cell-free DNA and the concentrations of CK-MB, troponin I and C-reactive protein. In serial specimens, we found that the cell-free DNA rose early, but peaked behind CK-MB. A slightly diffused DNA ladder could be found with pooled cell-free DNA from MI patients by electrophoresis with the smallest DNA band at only a few hundred base pairs. Conclusions: Cell-free DNA in MI patients is increased in patients diagnosed with MI, and may complement troponin and CK-MB in a multiple marker test format.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0009-8981
1873-3492
DOI:10.1016/S0009-8981(02)00337-6